Minato S
Clin Chim Acta. 1979 Mar 1;92(2):249-55. doi: 10.1016/0009-8981(79)90120-7.
A new colorimetric method for the serum enzyme assay was developed, using the color reaction of a ferrous salt complex and a primary aromatic amine. For this method new substrates containing primary aromatic amines were synthesized. The aromatic amine liberated by the enzyme reaction was measured by its color reaction with pentacyanoammineferroate treated with hydrogen peroxide. The determination was made at a wavelength of around 700 nm, at which the assay is not affected by colored substances in serum. Therefore a blank assay was not necessary. This method was applied to the assay of serum gamma-glutamyl transpeptidase, cystine aminopeptidase, and leucine aminopeptidase. The results obtained were in good agreement with those of the p-nitroanilide method also used to assay each enzyme. This new method can be used on a Technicon autoanalyzer system.
利用亚铁盐络合物与伯芳香胺的显色反应,开发了一种用于血清酶测定的新比色法。为此合成了含伯芳香胺的新底物。酶反应释放出的芳香胺通过其与用过氧化氢处理的五氰合氨合铁酸盐的显色反应来测定。测定在700nm左右的波长下进行,在此波长下该测定不受血清中有色物质的影响。因此无需进行空白测定。该方法应用于血清γ-谷氨酰转肽酶、胱氨酸氨肽酶和亮氨酸氨肽酶的测定。所得结果与也用于测定每种酶的对硝基苯胺法的结果高度一致。这种新方法可用于Technicon自动分析仪系统。